View source for Competitive inhibition

{{Short description|Interruption of a chemical pathway}}
{{Use dmy dates|date=July 2018}}
[[File:Ethanol-2D-flat.svg|thumb|[[Ethanol]] ({{chem|C|2|H|5}}{{chem|O|H}}) serves as a competitive inhibitor to [[methanol]] ({{chem|C|H|3}}{{chem|O|H}}) and [[ethylene glycol]] ({{chem2|(CH_{2}OH)_{2} }}) for the enzyme [[alcohol dehydrogenase]] in the [[liver]] when present in large amounts. For this reason, ethanol is sometimes used as a means to treat or prevent toxicity following accidental ingestion of these chemicals.]]
'''Competitive inhibition''' is interruption of a [[chemistry|chemical]] pathway owing to one [[chemical substance]] inhibiting the effect of another by competing with it for [[molecular binding|binding]] or [[chemical bond|bonding]]. Any [[metabolism|metabolic]] or [[chemical messenger (disambiguation)|chemical messenger]]<!-- Yes, that superset link target is intentional --> system can potentially be affected by this principle, but several classes of competitive inhibition are especially important in [[biochemistry]] and [[medicine]], including the competitive form of [[enzyme inhibitor|enzyme inhibition]], the competitive form of [[receptor antagonist|receptor antagonism]], the competitive form of [[antimetabolite]] activity, and the competitive form of [[poisoning]] (which can include any of the aforementioned types).

==Enzyme inhibition type==
In competitive inhibition of [[enzyme catalysis]], binding of an inhibitor prevents binding of the target molecule of the enzyme, also known as the substrate.<ref name="NIH CTT">{{cite web |title=Types of Inhibition |url=http://assay.nih.gov/assay/index.php/Types_of_Inhibition |publisher=NIH Center for Translational Therapeutics |access-date=2 April 2012 |url-status=dead |archive-url=https://web.archive.org/web/20110908030859/http://assay.nih.gov/assay/index.php/Types_of_Inhibition |archive-date=8 September 2011 }}</ref> This is accomplished by blocking the binding site of the substrate – the active site – by some means. The V<sub>max</sub> indicates the maximum velocity of the reaction, while the K<sub>m</sub> is the amount of substrate needed to reach half of the V<sub>max</sub>. K<sub>m</sub> also plays a part in indicating the tendency of the substrate to bind the enzyme.<ref name=":3">{{Cite book| vauthors = Lodish H, Berk A, Zipursky SL, Matsudaira P, Baltimore D, Darnell J |year=2000| chapter = Functional Design of Proteins | chapter-url= https://www.ncbi.nlm.nih.gov/books/NBK21733/|title = Molecular Cell Biology | edition = 4th }}</ref> Competitive inhibition can be overcome by adding more substrate to the reaction, which increases the chances of the enzyme and substrate binding. As a result, competitive inhibition alters only the K<sub>m</sub>, leaving the V<sub>max</sub> the same.<ref name=":2"/> This can be demonstrated using enzyme kinetics plots such as the [[Michaelis–Menten kinetics|Michaelis–Menten]] or the [[Lineweaver–Burk plot|Lineweaver-Burk plot]]. Once the inhibitor is bound to the enzyme, the slope will be affected, as the K<sub>m</sub> either increases or decreases from the original K<sub>m</sub> of the reaction.<ref name=":7" /><ref>{{Cite journal| vauthors = Eadie SG |year=1942|title=The Inhibition of Cholinesterase by Physostigmine and Prostigmine |journal=Journal of Biological Chemistry|volume=146|pages=85–93|doi=10.1016/S0021-9258(18)72452-6|doi-access=free}}</ref><ref>{{Cite book | vauthors = Berg JM, Tymoczko JL, Stryer L |year=2002| chapter = Appendix: Vmax and KM Can Be Determined by Double-Reciprocal Plots | chapter-url = https://www.ncbi.nlm.nih.gov/books/NBK22557/ | title = Biochemistry | edition = 5th }}</ref>

Most competitive inhibitors function by binding reversibly to the active site of the enzyme.<ref name="NIH CTT" /> As a result, many sources state that this is the defining feature of competitive inhibitors.<ref>{{cite web |vauthors=Ophardt C |title=Virtual Chembook |url=http://chemistry.elmhurst.edu/vchembook/573inhibit.html |publisher=Elmhurst College |access-date=1 September 2015 |archive-date=17 October 2015 |archive-url=https://web.archive.org/web/20151017064913/http://chemistry.elmhurst.edu/vchembook/573inhibit.html |url-status=dead }}</ref> This, however, is a misleading [[oversimplification]], as there are many possible mechanisms by which an enzyme may bind either the inhibitor or the substrate but never both at the same time.<ref name="NIH CTT" /> For example, allosteric inhibitors may display competitive, [[non-competitive inhibition|non-competitive]], or [[uncompetitive inhibition|uncompetitive]] inhibition.<ref name="NIH CTT" />

===Mechanism===
[[File:Comp inhib.svg|350px|Diagram showing competitive inhibition|right|thumb]]
In competitive inhibition, an inhibitor that resembles the normal substrate binds to the enzyme, usually at the [[active site]], and prevents the substrate from binding.<ref name=":1">{{Cite news|url=https://bio.libretexts.org/TextMaps/Map:_Biochemistry_Free_and_Easy_(Ahern)|title=Map: Biochemistry Free & Easy (Ahern and Rajagopal)|date=24 December 2014|work=Biology LibreTexts|access-date=2 November 2017}}</ref> At any given moment, the enzyme may be bound to the inhibitor, the substrate, or neither, but it cannot bind both at the same time. During competitive inhibition, the inhibitor and substrate compete for the active site. The active site is a region on an enzyme to which a particular protein or substrate can bind. The active site will thus only allow one of the two complexes to bind to the site, either allowing a reaction to occur or yielding it. In competitive inhibition, the inhibitor resembles the substrate, taking its place and binding to the active site of an enzyme. Increasing the substrate concentration would diminish the "competition" for the substrate to properly bind to the active site and allow a reaction to occur.<ref name=":2">{{Cite journal | vauthors = Berg JM, Tymoczko JL, Stryer L |year=2002|title=Enzymes Can Be Inhibited by Specific Molecules|url=https://www.ncbi.nlm.nih.gov/books/NBK22530/|journal=Biochemistry | edition = 5th }}</ref> When the substrate is of higher concentration than the concentration of the competitive inhibitor, it is more probable that the substrate will come into contact with the enzyme's active site than with the inhibitor's.

Competitive inhibitors are commonly used to make pharmaceuticals.<ref name=":2" /> For example, [[methotrexate]] is a chemotherapy drug that acts as a competitive inhibitor. It is structurally similar to the [[Cofactor (biochemistry)|coenzyme]], [[folate]], which binds to the enzyme [[dihydrofolate reductase]].<ref name=":2" /> This enzyme is part of the synthesis of DNA and RNA, and when methotrexate binds the enzyme, it renders it inactive, so that it cannot synthesize DNA and RNA.<ref name=":2" /> The cancer cells are thus unable to grow and divide. Another example: [[prostaglandin]] are made in large amounts as a response to pain and can cause inflammation. Essential fatty acids form the prostaglandins; when this was discovered, it turned out that these were actually very good inhibitors to prostaglandins. These fatty acids inhibitors have been used as drugs to relieve pain because they can act as the substrate, and bind to the enzyme, and block prostaglandins.<ref>{{cite journal | vauthors = Flower RJ | title = Drugs which inhibit prostaglandin biosynthesis | journal = Pharmacological Reviews | volume = 26 | issue = 1 | pages = 33–67 | date = March 1974 | pmid = 4208101 | url = http://pharmrev.aspetjournals.org/content/26/1/33 }}</ref>

An example of non-drug related competitive inhibition is in the prevention of browning of fruits and vegetables. For example, [[tyrosinase]], an enzyme within mushrooms, normally binds to the substrate, [[monophenols]], and forms brown o-quinones.<ref name=":4">{{cite journal | vauthors = Jiménez M, Chazarra S, Escribano J, Cabanes J, García-Carmona F | title = Competitive inhibition of mushroom tyrosinase by 4-substituted benzaldehydes | journal = Journal of Agricultural and Food Chemistry | volume = 49 | issue = 8 | pages = 4060–4063 | date = August 2001 | pmid = 11513710 | doi = 10.1021/jf010194h }}</ref> Competitive substrates, such as 4-substituted benzaldehydes for mushrooms, compete with the substrate lowering the amount of the monophenols that bind. These inhibitory compounds added to the produce keep it fresh for longer periods of time by decreasing the binding of the monophenols that cause browning.<ref name=":4" /> This allows for an increase in produce quality as well as shelf life.

Competitive inhibition can be reversible or irreversible. If it is [[reversible inhibition]], then effects of the inhibitor can be overcome by increasing substrate concentration.<ref name=":1" /> If it is irreversible, the only way to overcome it is to produce more of the target (and typically degrade and/or excrete the irreversibly inhibited target).

In virtually every case, competitive inhibitors bind in the same [[binding site]] (active site) as the substrate, but same-site binding is not a requirement.  A competitive inhibitor could bind to an [[allosteric]] site of the free enzyme and prevent substrate binding, as long as it does not bind to the allosteric site when the substrate is bound.  For example, [[strychnine]] acts as an allosteric inhibitor of the glycine receptor in the mammalian spinal cord and brain stem. Glycine is a major post-synaptic inhibitory neurotransmitter with a specific receptor site. Strychnine binds to an alternate site that reduces the affinity of the glycine receptor for glycine, resulting in convulsions due to lessened inhibition by the glycine.<ref>{{cite book |title= Pharmacology for Nurse Anesthesiology |veditors= Ouellette R, Joyce JA |year= 2011 |publisher= Jones & Bartlett Learning |isbn= 978-0-7637-8607-6 |chapter= Chapter 2. Pharmacodynamics: The Study of Drug Action | vauthors = Dick RM |url-access= registration |url= https://archive.org/details/pharmacologyforn0000ouel }}</ref>

In competitive inhibition, the maximum velocity (<math>V_\max</math>) of the reaction is unchanged, while the apparent affinity of the substrate to the binding site is decreased (the <math>K_d</math> dissociation constant is apparently increased). The change in <math>K_m</math> ([[Michaelis–Menten constant]]) is parallel to the alteration in <math>K_d</math>, as one increases the other must decrease.  When a competitive inhibitor is bound to an enzyme the <math>K_m</math> increases.  This means the binding affinity for the enzyme is decreased, but it can be overcome by increasing the concentration of the substrate.<ref name=":0">{{Cite book|title=Fundamentals of biochemistry : life at the molecular level| vauthors = Voet D, Voet JG, Pratt CW |isbn=9781118918401 |edition=Fifth |location=Hoboken, NJ |oclc=910538334 |date = 2016-02-29 }}</ref> Any given competitive inhibitor concentration can be overcome by increasing the substrate concentration. In that case, the substrate will reduce the availability for an inhibitor to bind, and, thus, outcompete the inhibitor in binding to the enzyme.<ref name=":0" />
[[File:Allosteric comp inhib 1.svg|350px|Competitive inhibition can also be allosteric, as long as the inhibitor and the substrate cannot bind the enzyme at the same time.|thumb]]

==== Biological examples ====
After an accidental ingestion of a contaminated opioid drug [[desmethylprodine]], the [[Neurotoxicity|neurotoxic]] effect of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine ([[MPTP]]) was discovered. MPTP is able to cross the blood brain barrier and enter acidic [[lysosome]]s.<ref name=":6">{{Cite book | vauthors = Sian J, Youdim MB, Riederer P, Gerlach M |year=1999| chapter = MPTP-Induced Parkinsonian Syndrome| chapter-url= https://www.ncbi.nlm.nih.gov/books/NBK27974/| title = Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th Edition}}</ref> MPTP is biologically activated by MAO-B, an isozyme of [[monoamine oxidase]] (MAO) which is mainly concentrated in neurological disorders and diseases.<ref name=":5">{{cite journal | vauthors = Herraiz T, Guillén H | title = Inhibition of the bioactivation of the neurotoxin MPTP by antioxidants, redox agents and monoamine oxidase inhibitors | journal = Food and Chemical Toxicology | volume = 49 | issue = 8 | pages = 1773–1781 | date = August 2011 | pmid = 21554916 | doi = 10.1016/j.fct.2011.04.026 | hdl = 10261/63126 }}</ref> Later, it was discovered that MPTP causes symptoms similar to that of [[Parkinson's disease]]. Cells in the central nervous system (astrocytes) include MAO-B that oxidizes MPTP to 1-methyl-4-phenylpyridinium (MPP+), which is toxic.<ref name=":6" /> MPP+ eventually travels to the extracellular fluid by a [[dopamine transporter]], which ultimately causes the Parkinson's symptoms. However, competitive inhibition of the MAO-B enzyme or the dopamine transporter protects against the oxidation of MPTP to MPP+. A few compounds have been tested for their ability to inhibit oxidation of MPTP to MPP+ including [[methylene blue]], [[5-nitroindazole]], [[norharman]], [[9-methylnorharman]], and [[menadione]].<ref name=":5" /> These demonstrated a reduction of neurotoxicity produced by MPTP.[[File:Michaelis-Menten plot competitive inhibition.svg|thumb|Michaelis–Menten plot of the reaction velocity (v) against substrate concentration [S] of normal enzyme activity (1) compared to enzyme activity with a competitive inhibitor (2). Adding a competitive inhibitor to an enzymatic reaction increases the K<sub>m</sub> of the reaction, but the V<sub>max</sub> remains the same.]][[File:Enzyme Inhibition lineweaver-burk plots.gif|thumb|Lineweaver-Burk plot, the reciprocal of the Michaelis–Menten plot, of the reciprocal of velocity (1/V) vs the reciprocal of the substrate concentration (1/[S]) of normal enzyme activity (blue) compared to enzyme activity with a competitive inhibitor (red). Adding a competitive inhibitor to an enzymatic reaction increases the K<sub>m</sub> of the reaction, but the V<sub>max</sub> remains the same.]] [[Sulfonamide (medicine)|Sulfa drugs]] also act as competitive inhibitors. For example, [[sulfanilamide]] competitively binds to the enzyme in the [[dihydropteroate synthase]] (DHPS) active site by mimicking the substrate [[4-Aminobenzoic acid|para-aminobenzoic acid]] (PABA).<ref>{{Cite news|url=https://www.nih.gov/news-events/nih-research-matters/how-sulfa-drugs-work|title=How Sulfa Drugs Work|date=15 May 2015|work=National Institutes of Health (NIH)|access-date=2 November 2017}}</ref> This prevents the substrate itself from binding which halts the production of folic acid, an essential nutrient. Bacteria must synthesize folic acid because they do not have a transporter for it. Without folic acid, bacteria cannot grow and divide. Therefore, because of sulfa drugs' competitive inhibition, they are excellent antibacterial agents.

An example of competitive inhibition was demonstrated experimentally for the enzyme succinic dehydrogenase, which catalyzes the oxidation of [[Succinic acid|succinate]] to [[Fumaric acid|fumarate]] in the [[Citric acid cycle|Krebs cycle]]. [[Malonate]] is a competitive inhibitor of succinic dehydrogenase. The binding of succinic dehydrogenase to the substrate, succinate, is competitively inhibited. This happens because malonate's chemistry is similar to succinate. Malonate's ability to inhibit binding of the enzyme and substrate is based on the ratio of malonate to succinate. Malonate binds to the active site of succinic dehydrogenase so that succinate cannot. Thus, it inhibits the reaction.<ref>{{cite journal | vauthors = Potter VR, Dubois KP | title = Studies on the Mechanism of Hydrogen Transport in Animal Tissues | journal = The Journal of General Physiology | volume = 26 | issue = 4 | pages = 391–404 | date = March 1943 | pmid = 19873352 | pmc = 2142566 | doi = 10.1085/jgp.26.4.391 }}</ref>[[File:Allosteric comp inhib 2.svg|350px|Another possible mechanism for allosteric competitive inhibition.|thumb]]

===Equation===
The Michaelis–Menten Model can be an invaluable tool to understanding enzyme kinetics. According to this model, a plot of the reaction velocity (V<sub>0</sub>) associated with the concentration [S] of the substrate can then be used to determine values such as V<sub>max</sub>, initial velocity, and K<sub>m</sub> (V<sub>max</sub>/2 or affinity of enzyme to substrate complex).<ref name=":7">{{Cite book | vauthors = Berg JM, Tymoczko JL, Stryer L |year=2002 | chapter = The Michaelis–Menten Model Accounts for the Kinetic Properties of Many Enzymes |chapter-url=https://www.ncbi.nlm.nih.gov/books/NBK22430/|title = Biochemistry | edition = 5th }}</ref>

Competitive inhibition increases the apparent value of the [[Michaelis–Menten]] constant, <math>K^\text{app}_m</math>, such that initial rate of reaction, <math>V_0</math>, is given by

: <math> V_0 = \frac{V_\max\,[S]}{K^\text{app}_m + [S]}</math>

where <math>K^\text{app}_m=K_m(1+[I]/K_i)</math>, <math>K_i</math> is the inhibitor's dissociation constant and <math>[I]</math> is the inhibitor concentration.

<math>V_\max</math> remains the same because the presence of the inhibitor can be overcome by higher substrate concentrations. <math>K^\text{app}_m</math>, the substrate concentration that is needed to reach <math>V_\max / 2</math>, increases with the presence of a competitive inhibitor. This is because the concentration of substrate needed to reach <math>V_\max</math> with an inhibitor is greater than the concentration of substrate needed to reach <math>V_\max</math> without an inhibitor.

===Derivation===
In the simplest case of a single-substrate enzyme obeying Michaelis–Menten kinetics, the typical scheme

:<chem> 
E + S <=>[k_1][k_{-1}] ES ->[k_2] E + P
</chem>

is modified to include binding of the inhibitor to the free enzyme:

:<chem> 
EI + S <=>[k_{-3}][k_3] E + S + I <=>[k_1][k_{-1}] ES + I ->[k_2] E + P + I
</chem>

Note that the inhibitor does not bind to the ES complex and the substrate does not bind to the EI complex.  It is generally assumed that this behavior is indicative of both compounds binding at the same site, but that is not strictly necessary. As with the derivation of the Michaelis–Menten equation, assume that the system is at steady-state, i.e. the concentration of each of the enzyme species is not changing.

: <math chem>\frac{d[\ce E]}{dt} = \frac{d[\ce{ES}]}{dt} = \frac{d[\ce{EI}]}{dt} = 0. </math>

Furthermore, the known total enzyme concentration is <math chem>[\ce E]_0 = [\ce E] + [\ce{ES}] + [\ce{EI}]</math>, and the velocity is measured under conditions in which the substrate and inhibitor concentrations do not change substantially and an insignificant amount of product has accumulated.

We can therefore set up a system of equations:

{{NumBlk|:|<math chem> [\ce E]_0 = [\ce E] + [\ce{ES}] + [\ce{EI}]</math>|{{EquationRef|1}}}}

{{NumBlk|:|<math chem> \frac{d[\ce E]}{dt} = 0 = -k_1[\ce E][\ce S] + k_{-1}[\ce{ES}] + k_2[\ce{ES}] -k_3[\ce E][\ce I] + k_{-3}[\ce{EI}] </math>|{{EquationRef|2}}}}

{{NumBlk|:|<math chem> \frac{d[\ce{ES}]}{dt} = 0 = k_1[\ce E][\ce S] - k_{-1}[\ce{ES}] - k_2[\ce{ES}] </math>|{{EquationRef|3}}}}

{{NumBlk|:|<math chem> \frac{d[\ce{EI}]}{dt} = 0 = k_3[\ce E][\ce I] - k_{-3}[EI] </math>|{{EquationRef|4}}}}

where <chem>[S], [I]</chem> and <chem>[E]_0</chem> are known.  The initial velocity is defined as <math chem>V_0 = d[\ce P]/dt = k_2 [\ce{ES}]</math>, so we need to define the unknown <chem>[ES]</chem> in terms of the knowns <chem>[S], [I]</chem> and <chem>[E]_0</chem>.

From equation ({{EquationNote|3}}), we can define ''E'' in terms of ''ES'' by rearranging to

: <math chem> k_1[\ce E][\ce S]=(k_{-1}+k_2)[\ce{ES}]</math>

Dividing by <math chem>k_1[\ce S]</math> gives

: <math chem> [\ce E] = \frac{(k_{-1}+k_2)[\ce{ES}]}{k_1[\ce S]} </math>

As in the derivation of the Michaelis–Menten equation, the term <math>(k_{-1}+k_2)/k_1</math> can be replaced by the macroscopic rate constant <math>K_m</math>:

{{NumBlk|:|<math chem> [\ce E] = \frac{K_m[\ce{ES}]}\ce{[S]} </math>|{{EquationRef|5}}}}

Substituting equation ({{EquationNote|5}}) into equation ({{EquationNote|4}}), we have

: <math chem> 0 = \frac{k_3[\ce I]K_m[\ce{ES}]}\ce{[S]} - k_{-3}[\ce{EI}] </math>

Rearranging, we find that

: <math chem> [\ce{EI}] = \frac{K_m k_3[\ce I][\ce{ES}]}{k_{-3}[\ce S]} </math>

At this point, we can define the dissociation constant for the inhibitor as <math>K_i = k_{-3}/k_3</math>, giving

{{NumBlk|:|<math chem> [\ce{EI}] = \frac{K_m[\ce I][\ce{ES}]}{K_i[\ce S]}</math>|{{EquationRef|6}}}}

At this point, substitute equation ({{EquationNote|5}}) and equation ({{EquationNote|6}}) into equation ({{EquationNote|1}}):

: <math chem> [\ce E]_0 = \frac{K_m[\ce{ES}]}\ce{[S]} + [\ce{ES}] + \frac{K_m[\ce I][\ce{ES}]}{K_i[\ce S]}</math>

Rearranging to solve for ES, we find

: <math chem> [\ce E]_0 = [\ce{ES}] \left ( \frac{K_m}\ce{[S]} + 1 + \frac{K_m[\ce I]}{K_i[\ce S]} \right )= [\ce{ES}] \frac{K_m K_i + K_i[\ce S] + K_m[\ce I]}{K_i[\ce S]}</math>

{{NumBlk|:|<math chem> [\ce{ES}] = \frac{K_i [\ce S][\ce E]_0}{K_m K_i + K_i[\ce S] + K_m[\ce I]}</math>|{{EquationRef|7}}}}

Returning to our expression for <math>V_0</math>, we now have:

: <math chem> V_0 = k_2[\ce{ES}] = \frac{k_2 K_i [\ce S][\ce E]_0}{K_m K_i + K_i[\ce S] + K_m[\ce I]} </math>
: <math chem> V_0 = \frac{k_2 [\ce E]_0 [\ce S]}{K_m + [\ce S] + K_m\frac{[\ce I]}{K_i}} </math>

Since the velocity is maximal when all the enzyme is bound as the enzyme-substrate complex, <math chem>V_\max = k_2 [\ce E]_0</math>.
Replacing and combining terms finally yields the conventional form:

{{NumBlk|:|<math chem> V_0 = \frac{V_{\max}[\ce S]}{K_m\left(1 + \frac{[\ce I]}{K_i}\right) + [\ce S]}</math>|{{EquationRef|8}}}}

To compute the concentration of competitive inhibitor <chem>[I]</chem> that yields a fraction <math>f_{V{_0}}</math> of velocity <math>V_0</math> where <math>0 < f_{V{_0}} < 1</math>:

{{NumBlk|:|<math chem> [\ce I]= \left(\frac{1}{f_{V{_0}}} -1\right)K_i\left(1+\frac{[\ce S]}{K_m}\right)</math>|{{EquationRef|9}}}}

== See also ==
*[[Schild regression]] for ligand receptor inhibition
*[[Non-competitive inhibition]]

== Notes and references ==
{{Reflist|30em}}

{{Enzyme inhibition}}

[[Category:Enzyme inhibitors]]